Canonical Allele Identifier: CA653388099

Gene: CHST3

Linked Data

• COSMIC: COSN20919535

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72010141_72010142insG , CM000672.2:g.72010141_72010142insG	GRCh38
NC_000010.10:g.73769899_73769900insG , CM000672.1:g.73769899_73769900insG	GRCh37
NC_000010.9:g.73439905_73439906insG	NCBI36
NG_012635.1:g.50780_50781insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1670_*1671insG MANE Select	ENSP00000362207.4:n.*1670_*1671insG
ENST00000373115.4:c.*1670_*1671insG	ENSP00000362207.4:n.*1670_*1671insG
NM_004273.4:c.*1670_*1671insG	NP_004264.2:n.*1670_*1671insG
XM_006718075.2:c.*1670_*1671insG	XP_006718138.1:n.*1670_*1671insG
XM_011540369.1:c.*1670_*1671insG	XP_011538671.1:n.*1670_*1671insG
XM_006718075.4:c.*1670_*1671insG	XP_006718138.1:n.*1670_*1671insG
XM_011540369.2:c.*1670_*1671insG	XP_011538671.1:n.*1670_*1671insG
NM_004273.5:c.*1670_*1671insG MANE Select	NP_004264.2:n.*1670_*1671insG